Substance for treatment of tuberculosis, leprosy, and other diseases and process of mixing said substance.



I UNiTED 7 STATES ATENT OFFICE,

BENJAMIE s AsGH LL, or SEATTLE, WASHINGTON.

SUBSTANCE ron TREATMENT or ToianncnLosls, LErnosY, AND OTHER nIsEAsEs Ann PROCESSOR MIXING SAID sUes ancE.

No Drawing.

To all whom it may concern:

Be it known that 1,.BEN JAMIIN S .Piiso1-nuin, a citizen of the United States, and a resident of Seattle, State of Washington, have in vented certain new and useful Improvements in Substances for Treatment of Tuberculosis, Leprosy, and other Diseases and Processes of ll/[alring Said Substances, of which the followingis aspecification.

This invention relates to a new method of treating and raising the immunity against tuberculosis, leprosy and other diseases, based upon hitherto unknown blo-chemical phenomena, and by means of a new substance 'high, molecular complexity.

produced by a new process. As a part of the process for producing the new substance, my inyentii'in also relatesfor growing the bacilli, which media is duced by a new process.

It has already been stated in my copencb proing application, Serial No. 784:,706, that antibodies enzyms of specific nature-are produced by animals and man following the introduction, artificially or otherwise, of certain substances of more or less, usually The specific enzyme are capable of cmnbining,- with the substance introduced. in such a manner as to bring about its alteration for purposes of assimilation or destruction, as the c; numbe.

In the present state of our knowledge, the relationship between, the delense mechanism of living p rotoplasm and its metabolic functions lies in exceedingly close parallelism, the main difference seeming to be one of specificity, thoughit is well recognised that the :t'unctions are so similar that the terms enteric and parenteric enzyme are of constant application. My researches and discoveries to new culture media phin, renders them inert.

Specification bf Letters Patent. Pat t d D c. 18, 1917, Application filedMay 1, 1917. Serial m5. 165,710. i l

compo'lu'uls the physiological action may be proi'rumdly altered by the addition to or.

substitution of, in the first series, the hydrocarbon chain with alkyl, hydroxyl, carbonyl, carbonyl, sul'fonal or ammo groups, the

halogens, etc, while in the second series the latent action of the nucleus is profoundly altered by both the presence and the position of these and an infinite number of other groups existing as side chains or in chemical combination.

As a result of my researches and experiments, I may state that in general while the introduction of certain of these groups into.

the molecule of certain drugs and other compounds, of like nature and more or less s mple structure, often renders them useless,

' inert and of Wholly different physiological action, the same does not necessarily follow in the more complex moleculesaboutto-be described, as far as antibody formation is concerned, indeed I have discovered the reverse to be frequently the case. For instance, from a iiharmacological standpoint, the entrance of carboxyl into methylamin changes the latter into a harmless glycin. Sulfonation of many bodies, as for examplc mor Active aldehydcs become inactive aldols by the introduction of the hydroxyl group and poisonous alcohols become harmless glycerols and mannitols by the same process. Further more, the selective action of adrug depends upon both the'definite structure of the parent molecule aswell as this specific allinity of its side chains for certain groups of cells in the body. The selective action of cocaine for ner\-'e-e1:1dings is Well known, and masking the carbonyl group of benzoyl ecgonin brings this about. Trional, sulfona-l and other compounds of this series are mercaptan derivatives containing the alcohol vgroup as a sl'le chain, the sleep-producing effect of the drug being due tothe fact that the alcohol cannot be oxidized by any body-cell, but is only liberated in the sleep centers of the brain. h Now, approximately the same quantity oil: alcohol attached to another molecule, a Xanthin molecule, for example (cafl'ein) becomes a powerful heart stimulant and diuretic.

The action of a pharmaceutical compound.

cule, which poisonous substance becomes liberated at the momentthe side chain portion of the derivative attaches itself to the organism in question, causing its destruction, without-combining with the body 'cells' of the host and exerting its poisonous action. upon them. These are fundamental prlnciples underlying the relationship which exists between chemical composition and pharmacological action. In my researches, experiments and discoveries, I have utilized the foregoing principles for the production of pharmacological action and chemotherapeutic properties and have combined them with the principles ordinarily understood to overn the production ofimmunity in the following way. Much of the synthetic chemistry of the cyclic compounds is simply an elaboration or modification of the benzol nucleus C H from which hydrocarbon, countless new substances have'been built up in the laboratory. In a like manner have built up many new. synthetic substances using instead of benzol the various unsaturated hydrocarbonselaborated by the tubercle bacillus, and in like manner have added appropriate side chains or combining groups by identical-processes, so that'the hydrocarbons thus acted upon maybe so modified as to be taken up by the -body cells when properly introduced whereupon immunity for all the original hydrocarbons from I which the derivatives come will take place when all its ingredientsare present, .provided these changes have been brought about without disturbing or altering in any Way the basic configuration of the original molecules (isomerism, polymerization, etc.)

In my copencling application, Serial No.

784,706, I stated that a considerable degree of immunity could be produced by the in-' troduction into the blood of the ethyl esters of the fatty acids obtained from the wax of the tubercle bacillus. My subsequent researches have developed the fact that this immunity can be very greatly enhanced by the production of suitable combinations,- (artificial addition of side chains), with the various other portions of the wax. These derivatives consist of unsaturated hydrocarbons and alcohols in addition to the. fatty tion,

acids originally described.- In passing, it

may be said that the origin of these hydrocarbons is somewhat in doubt, it being well known that some unsaturated alcohols readily pass into olefins on heating in presence of alkalis, etc., though the original wax isinsoluble in acetic anhydricL-andwhile on account of their natural reactivity they already have a slight natural immunizing value, their activities are very considerably enhanced by condensation or combination with other suitable substances, as for example, with certain aldehydes, ketones and organic acids of either the aliphatic or cyclic series. It is probable that these hydrocarbons either exist free, as is the case in certain other waxes, in oil of roses,-in the terpenes and in various other places 1n nature,

or that they exist in chemical combination with fatty acids present in the tubercle bacillus Wax and are split free'during the process of saponification, the latter view being the most likely, since 'upon saponification of a synthetically formed ester, I usually recover the hydrocarbom It seems, however, that the various naturally occurring Wax esters, e., the hydrocarbons and alcohols, especially the former, in their original combination with the fatty acids are exceedingly hard to split by the body-unless The higher modified as I will describe. alcohols which may be esterified to form suitable esters as the acetates, lactates, benzoates, salicylates, etc., are far less reactive before this treatment, even though they possess an active OH group, and absorption in the tissues ismanifestly much slower and in some cases fails to take place at all.

I have observed that the saponification process alone 1s by far the most important slngle step in effecting a separation of the yarious molecular complexes of the wax,

since after saponification, any of these substances, hydrocarbons, alcohols, acids, or all of them are more readily taken up by the tissues than before hydrolysis had taken place, whereas, if the saponification .is incomplete, failure on the part of the tissues to combine and take up the wax is immediately evident. The esterification or condensat-ion of hydrocarbons, alcohols and fatty or fatty acids in some suitable manner is also a 'very necessary step, of the process,

in that it protects thesemolecules from further chemical changes, (oxidation, tion, and especially polymerization). densation of thehydrocarbons with suitable substances or direct esterification, halogenation or oxidation and subsequent esterificaor substitution of the derivative, etc., render it more stable and enormously enhance its capacity for combining with suitable body cells (receptors). Now, while in theory the injection of the recombination, reduc- Conhydes into fatty acids with physical mixture,

blood and tissues these anti enzyme will attack and break up about immunity.

wax of the tubercle bacillus into the those of others, that such a phenomenon does not take place, on account of the ex treme stability of the parent molecule. lVhen, its various parts and each of these parts combined with other suitable chemical substancesor transformed into more suitable chemical bodies, 11. 6., hydrocarbons into alcohols, alcohols into aldehydes and aldetion or esterification products,"which act as intermediaries between various wax derivatires and the body cells, and these-parts are remixed in the same proportion as they existed in the parent substance in the simple but so alteredor modified as to be suitable for injection, it will then be found, as has been proved by my researches and discoveries that the body cells will produce antibodies (enzyme) for all the different esters," condensation products or other suitable transformation "complexes,

which anti-bodiesare specific in turn for the :parent substance, that is the original tubercle bacillus wax, and after reaching a suiiicient degree of concentration in the bodies or the hitherto unattached parent substance, that is the wax surrounding the living tubercle bacillus whereby disorganization, together with the destruction of the micro-organism and the disappearance of the" disease ensues in ;consequence. Previous to my researches and discoveries no investigator has sought to attach actual chemical side chains to the various antigens by following Quttheprin-H ciples which are applied in the production of synthetic drugs and other chemotherapeutic substances, in order that the antigen itself may be supplied with chains exactly as pliarm'acophore groups are attachedto bring about a specific action of the synthetic drug in question. Nor, has anyone demonstrated or-even suggested the possibility that antigens (chemical substances produced by invading micro-organisms) could be so treated in order to bring These researches and dis coveries therefore embody a basic principle not hitherto known to exist.

It should be understood that the words side chain as used" by the chemist to denote very definite chemical formulae of 7 known molecular composition are used by the innnunologist as urely diagrammatic imaginary bodies of un mown chemical com- I 1 position and little understood action, a term however, this molecule is split into their condensa- 7 suitable side found out about the ultimate composition of these combining groups possessed in common by body cells and bacteria.

Previous to my 1nvestigations and discoveries, the production of tubercle bacillus waxrapidly and in large quantities and at a very moderate cost was unknown. The market cost of a pound of the dried tubercle bacillus from whicha third to a half of a pound of the wax can be obtained, ranges from seven hundred and fifty ($750.00) dollars to one thousand ($1,000) dollars. My

incubator, which serves as a model, has a capacity about 220 cubic feet, andproduces on an average of five pounds of dried tubercle bacilli per month. In order to do this, Ifirst discovered that certain attenuated fast growing tubercle bacilli or other.

acid fast organisms belonging to'the same group produce, waxes of approximately the same chemical composition as is produced by a highly virulent and very slow growing tubercle bacillus. media used by others for growing the tubercle baccilli andother acid fast organisms belonging to this series, (lllycobactcriacere) consist of extract of-beef, peptone, glycerin and salts, and one gallon of this media 1 grown with virulent tubercle bacilli yields from one to three. grams of dried organisms in from'three to six months, at. a cost of approximately one dollar per "gallon, for

The classical culture culture media used, while with my new media to be described, I obtain a yield of.

from fiv'e to ten grams dried tubercle bacilli in from three. to six weeks at a cost of approximately one cent a gallon or less. It

will thus readily be seen thatthe cost of. methods used by others will production by render it wel nigh prohibitive. This cheap 'culture media therefore, I consider one of the most important discoveries inthe process and "while other inexpensive culture media have been used successfully by myself, the ones I am about to describe are the 1 ones I prefer. These organisms demand for their growth chiefly, four kinds of chemical substances, salts, extractives, proteids and a suitable source of carbon (carbohydrates or hydrocarbons) for wax-building. 1 obtain my extractives and part of my proteids from brewers or distillers yeast, chemical analysis having shown a close identity between the extractives from yeast and beef. For mypi'oteids Iuse dried skim milk or other cheap proteids which are not denatu-alized rendered unsuitable for the growth of micro-organisms) by the action of chemicals,- (acids or alkalis which areused in lieu of the expensive digestive ferments for the production ofhydrolysis) (peptones); I,

treat dried skim milkwith such an amount of caustic potash or soda that it becomes soluble in water so as to produce a neutral solution after heating, (not a colloidal suspension). As a source of carbon for wax building, I use glucose-which must not be added to the milk soda solution until after it becomes neutral, 5.6., until chemical combination has become Ycomplete. Brewers yeast is treated with, approximately 7 KOH "or NaOH and boiled for several days before hydrolysis is complete. A calculated .quant-ityJof this solution is then added to the milk powder, so that the end reaction is 'neu'tralor slightly acid.- In case of-distillery-waste, a mineral acid preferably hydrochloiic is used unless the sugar-content is so low as not to injure the culture media to greatly increase the quantity of organisms.

grown without disturbing in. any way the chemical composition ,ofthe. wax elaborated byfthebacillus. As amatter of-fact, my researches have proved time andagain that the additioirof glycerinhas a tendency to increase the production of fatty acid glycerids at the expense of morevaluable higher a-lcohols'and hydrocarbons. I also claim as a new discovery the use of rapidly growing tubercle bacilli aswell as of the other acidfast organisms as timothy. bacilli, butter bacilli, grass bacilli, e'tc., and have proved by analysis that the wax elaborated by them is identical. with that produced by yirulent tubercle-bacilli. It is also important for" my. process that the culture media be frequently shaken during the growth of the or-. ganism, at least once a week or once in ten days, the chemical composition of the wax being profoundly affected bythis procedure. The well-known fact that attenuated tubercle bacilli or other acid-fast organisms do not produce the same toxins (tub'ercu lins) which are produced by virulent organisms, does not follow out when it comes to the production of waxes, asI have proved byehemical analysesandby experiments onanimals, The suitable proportions of-the various wax ingredients as hasbeen shown by the an'alysis'of the virulent tubercle bacilli, are approximately hydrocarbon derivatives two parts, higher alcohol esters one part and esters of fatty acids three parts. I also consider as important the selection of certain strains of organisms which produce the suitable waxes ,in suitable proportions and which in addition produce dry clumping growths on cheap culture media and not easily broken up-in the process of separatingthem from the culture media upon which they grow, and thus entailing great loss of bacillary substanceon straining and subsequentwashing. After complete growth is obground in a suitable grinding machine. They are then placed in an alcoholic potash solution'containing an excess of chemically pure potassium"hydroxid in 96% alcohol. Equal parts of benzol may be added and the whole subject to saponification under a'refiux condenser. In this the saponifyingmedium should be kept about 80? centigrade, free from air and should be supplied with a mechanical stirrer and saponifled from twelve to twenty-four hours. I

consider it important that the temperature I of the sa'ponifying media doesfnot exceed 80 centigrade. After saponificatlon, which is complete in about twelve to twenty-four hours, thesupernatant fluid is decanted and the residue is washed in alcohol and-benzol and the washings added to the decantedv liquid. Equal parts of water are now added, and if necessarv, the caustic potash. nearly neutralized with a dilute acid or CO gas. This solution which shouldbe kept moderately cool, not exceeding 80 C., is shaken with hot benzol in a suitable container. lVith this treatment the benzol containing the hydro-carbons and alcohols will separate into .a supernatant layer with the soluble soaps beneath. The soap solution is washed twice more with benzol and the benzol fractions united. Benzol fractions are partly concentrated by distillation in cacao and washed with water containing alcohol and this is continued back and forth'until the benzol is free from soaps and contains only hydrocarbonsand alcohols and the wash-- water contains only soaps. During this process the absence of air is desirable but not imperative. The dilute alcoholic alkali solution now contains substantially all the potassinm salts of the fatty acids present in the tubercle bacilli ranging from about 25% to about 45% of the total substance .by weight originally treated. The whole is then treated with dilute acid, as hydrochloric or sulfuric acid, whereby the insoluble fatty acids are precipitated. These insoluble fatty acids are collected on a filter, washed, dried and dissolved in five to ten times their quantity of ethyl alcohol, filtered and esterified by the addition of an excess 'of sulfuric acidor by passing anhydrous \hydrochloricacid gas through the mixture for about an hour. The resulting esters arenow washed in hot water until free from acid and are ready for use. The ethyl esters derived from the tubercle bacillus wax are a dark brown oil or fat-like substance, solid'at room temperature, possess mg a fruit-like fragrant order and resinous,

slightly blirning taste, liquefying at from about 25 to about 35 G., theresulting liquid 'ibeing of a clear dark color, insoluble in water and possessing a neutral reaction. It is soluble in ether, chloroform and petroleum ether, insoluble in glycerin and sparingly sdluble in alcohol. Aqueous mineral acids and alkalis decompose it into its fatty mination of these. .trated ammoma yields the am1ds.

acids and its identification may be determined by hydrolysis and subsequent deter- Treatment with concen- These esters distil between about 250 C. and about 350 C. withmore or less decomposition. The specific gravity of the esters isqabout .86 to .89. The bcnzol portion is now distilled preferably in vacuum, until the benzol is mostly removed. Dilute glacial acetlc acid or preferably hydrochloric acid which removes traces of proteid is now. added in considerable quantity until the mixture is weakly acid, drawn oil from the benzol and the distillation continued in oaouo until no more benzol comes off. The alcohols and hydrocarbons are now"dried, treated with equal parts of acetic anhydrid and boiled under a reflux condenser for two hours. The mixture is then placed in a separatory funnel, cooled "to, about 37 (1., and the acetates of higher alcohols dii'awn oil. A second treatment 'using a little more acetic anhyconsiderably.

a gummy mass. The excess of chlorin and the ,chlorin in the addition products may be removed by shaking the petroleum ether in hot water containing potassium or silver acetate several hours. The petroleum ether is then evaporated ata low temperature in a vacuum and the now purified acetic esters of the higher alcohols recovered, although .the method of bleaching which I prefer when practical is by direct sunlight on the alcohol acetates, they being exposed severaldays in thin layers and subsequently filtered.

The hydroca'irbons are now purified by boiling in acetone (about five times the quantity) and decantind' the latter at about 37.

(1., and repeating this until the acetates of the remaining higher alcohols have been removed, as may be shown bytheir solubility in warm acetic anhydrid. The now purified hydrocarbons may be treated in one of several ways. They may be placed in an excess of carbon tetrachlorid' and bromin cautiouslyyaddedat room temperature until decolorization no longer takes place after standing several hours. An excess of silver acetate is then added and heat applied, whereupon the acetates of the alcohol derivatives of the hydrocarbons may be obtained. Or, the hydrocarbon may be oxidized in dilute potassium permanganate sulfuric acid solution and the oxidation products (alco' hols) subsequently esterified. They maybe oxidized by heating with dilute nitric acidand by treating with acetic acid in the presence of dilute sulfuric acid, but the method which I prefer is as follows :-The hydrocarbons are dissolved in five times the quantity of chloroform or carbon tetrachlorid and heated with equimolecular propor-.

tions of sodium salicylate and about onethird molecular proportion of phosphorous penta-chlorid, and the wholeheated at'a low temperature for twenty-four hours and the CCL; distilled'ofl, or the GU1 may be omitted and the mixture directly heated to 130 C. for thirtyminute's. The salicylates are then poured ofl flrom the residue purified by washing with dilute alkali until neutral, dr ed at low temperature and are ready for use. The melting point of the mixed hydrocarbons is from 55 to 60 (1., and the melting point of the salicylates'is 38 to 40. The salicylic esters of the hydrocarbons are now mixed with acetic esters of higher alcohols in about the proportion of two to i one, and these in turn are mixed with an equal, proportmn of the ethyl esters of the fatty acids, described as above or in Serial No. 784,706. I have also used with equalsuccess in treating tuberculosis the salicylic esters .of both alcohols and hydrocarbons madeby the identical steps described for the hydrocarbons alone. Previous to my researches, however, no one has succeeded in combin'mg unsaturated hydrocarbons direct with fatty acids by the use of PS1,, although the method has been used frequently in the case of alcohols of both series. Indeed, so rare are higher unsaturated hydrocarbons of this aliphatic series, that almost nothing is known about their'behavidr, either chemically or biologically. 1

The substance most closely related belong to the terpenes, the essentialo'ils and a few unsaturated compounds ofthis class obtained in the laboratory synthetically.- In all my 1 experimental work, therefore, I have had ht lecr nothing on which to base my observationsfrom those which had been made previously by other upon very similar compounds.

I consider it important for my process that these hydrocarbons be furnished with just as many OH groups as is practicable and these in turn united to as many appropriate side chains as is possible, always bearing in mind that while the addition of each OH group increases the ease of absorption and assimilation by the tissue and cells of the body, it also increases the difficulty of hypodermic administration, it being found that the oillike characteristics of the substance decrease and the sugar-like properties increase (increase of solubility in the body fluids) in just the-plopol'ti0n that the OH groups are contained in the molecule. In other words, I have observed all the transitional stages between hydrocarbons and carbohydrates,

with these highly reactive-bodies in the laboratory and the ease or ditliculty of injection is an important criteria.

The substances thus produced, resemble, more thananything else, the wax ot' the tubercle bacillus, although the melting point is somewhat lower and the mixturefpossesses a quite definite, somewhat fragrant odor. Its color depends upon the degree of purification, certain methods of bleaching, and the'care with which the oxygen and other impurities have been excluded at certain periods of its production. As a means of identification, inaddition to the characteristics about to be described, it is claimed that this substance possesses specific characteristics; z. 0., it conforms with the laws commonly understood by biologists and gen erally recognized by workers in the field of immunity. For example, human red blood corpuscles will produce, in an experimental animal, specific ferments capable of. dissolving human red blood corpuscles and not capableof dissolving red blood corpuscles of an other species of animal, exceptthose closely related to or identical with the human species. That is, the'serum of a guinea pigpr rabbit thus treated will, after an interval digest human blood corpuscles, but not those of an oX, (log, sheep, goat, or pig.

Furthermore, in the standardization of diphtheria antitoxinfthe test animals are first injected with lethal doses of diphtheria toxin, or many times the lethal dose, together with the antitoX-in. Since the chemi cal nature of antitoxin is unknown, its chief means of identification, potency and. specificity depends on this single characteristic, namely, that it and no other known substance will prevent the death of the ani mal receiving lethal doses of diphtheria. toxin. Furthermore, no other antitoxin, like tetanus antitoxin has the slightestefi'ect in neutralizing diphtheria toxin.

1n the practical manufacture Qf this subthis method and that ofstandardizing diphorganisms in sui'licient amounts to destroy held in solution stance for the treatment or tuberculosis in man, a portion of each manufactured lot or batch produced is set aside and used on .a guinea pig artificially inoculated with virulent fatal doses of tubercle bacilli. It the substance herein described fails to act and the animal dies otthe disease, the whole output or batch is discarded and not used for human treatment. The similarity between theria antitoxin becomes at once evident.

So faras known, no other substance so far discovered will eradicate tuberculosis in a susceptible animal inoculated with virulent so life in approximately ninety days, as I claim takes place with this substance. Any other substance which producesthis result should, according to our present conception of immunity, be identical in chemical structure to the one herein described. Also, characteristics for identification may be found in the original wax from which it is derived, this laborious process. of growing these organisms and extracting the waxes therefrom being the only known method of obtaining this particular parent substance. For example, a guinea-pig inoculated with 5/l00. milligrams of virulent tubercle bacilli will die in from 6 to 12 weeks in a vast majority of cases, whereas a similar animal inoculated with the same dose and treated with proper doses at suitable intervals with the derived substances herein described will completely recover from the disease in the vast majority of cases. Furthermore, the processes herein described for the production of substances easily absorbed by the, tissues are in many instances the identical processes used by chemists for purposes of identification of the various fats and waxes.

Analysis of the original waX develops the presence of two unsaturated hydrocarbons, two unsaturated alcohols, and four unsaturated. fatty acids. The hydrocarbons have a bromin absorption value'which will indi cate a molecular Weight corresponding to approximately C l-l (40%) and C H (3 76). the melting point of one hydrocarbon is 65 C. and the other one 55- C. They and 115 their alcohol derivatives are insoluble in twice the quantity of boiling acetic anhy drid, a distinction from all other known. higher alcohols. Conversion of the hydrocarbons into alcohols slightly increases their solubility in acetic anhydrid, but doesnot render them wholly soluble, even in large quantities of boiling acetic anhydrid. They are insoluble in even five times the quantity of acetone at 37 (3., the naturally occurring esters, being almost wholly at this temperature. They may be converted intoalcohols by many of the known methods of oxidation, although a great number of the commonly employed .130

alcohols, or their methods (sulfonation, halogenation, etc.,) yield resinous polymerization products or carbohydrates. The salicylates of the mixed hydrocarbons as I use them, are clear, lightcolored, somewhat viscous substances, having a melting point of about 38 C. Saponification of the salicylates' recovers salicylic acid in such quantity as to prove equimolecular combination, and the hydrocarbons are recovered from the saponification mixture. This fact alone strongly indicates the presence of the hydrocarbons in the original Wax. No investigator has hitherto effected a direct esterification of unsaturated hydrocarbons by the methodI have described. The classical methodof Bertram causes unsatisfactory polymerization products. By the action of strong alkalis these hydrocarbons form addition products which are in turn decomposed by water, whereby the melting point becomes raised 40 or (3.,

V and on additionof dilute acid or water they 'rid,-benzoyl chlorid, etc., (further differentiating from alcohols). Upon oxidizing the hydrocarbons with dilute potassium p'erman ganate in the presence of sulfuric acid and boiling with twice the quantity of acetic anhydrid, an acetate isiormed with a melting point of 58C. Tests for aldehydes have been negative, e., the compounds do not form compounds with saturated sodium bisulfite, do not react with phenlyhydrazin, or hydroxylamin hydrochlorid, do not color the fuchsin reagent, etc. The hydrocarbons are polymerized bymany of the metallic salts, as ZnOl A161 Fe,(Cl) etc., even in traces. (That is the reason why chemically pure reagents must be used in these rocesses as well. as, suitable containers.)

eating thefhydrocarbons with fuchsin or fuchsin decolorized with acid gives a very dark purple color, (not decolorized by ethyl alcohol), while the alcoholsv or their ,acetates are dyedred, a matter of great bio chemical importance,since the resting, forms or spore forms of the tubercle bacilli, give the deep purple red color, while the activity growing organism stains red, from which it may be concludedthat the most resistant forms of tubercle bacilli chiefly utilize the hydrocarbons for their protection. The specific gravity of the hydrocarbons is 0.84062.

adding an excess of silver acetate and warm.

ing for twenty-four hours under a reflux condenser, filteringand evaporating the solvent. Saponification of these acetates shows equimolecular combination to have taken place. They, however, are only sparingly soluble in boiling acetate anhydrid, a peculiarity which would serve to difi'erentiate them from other up to now described higher alcohols. I

The two alcohols, or their acetates, are soluble in twice the quantity of acetic anhydrid or five times the quantity of acetone cooled to 37 C. They are very dark in color, due to impurities, (hydrocarbons boing light in color), and readily polymerize inthe presence of strong alkalisor acids,

traces of metallic salts, and other impurities,

etc., from which the original alcohols can not be regenerated. By fractional crystallization from acetone, these alcohols may re solve into two portions, one having a melt ingpoint 50 0., and one having a melting point 10 C. The melting point of the acetate of higher fraction is 45 C. Sap0nification of this fraction givesan acetyl value of 100.98 corresponding to molecular weight I.. Q II O (408). The acetates of the fraction melting at 10C, occur in very small quantities. They do not combine with metals and probably difier from the hydrocarbons in containing a double bond. (olefins).

These alcohols are easily de'colorized by passing chlorin through their solution in C(ll,for'.-.petroleum ether and evaporating over sil ver'or potassium acetate or by exposure to sunlight in thin layers. The melting point of all the various. derivatives mixed together, is approximately 35 and contains in suitable proportions suitable esters or condensation products of the hydrocarbons, together with suitable esters or condensation products'of the higher alcohols in addition to suitable proportions offthe ethyl esters of the fatty acids described as above'or in my previous application, Serial hTo. 784:,706. This substance, as before mentioned, is most useful when its parts are mixed together in the proportion .of esters of hydrocarbons'two; esters of alcohols, one; ethyl esters of fatty acids, three.

Analysis of the original wax in my laboratory gives:

Iodin value; 20 Saponification. value -l 130 V Unsaponifiable substance -.33 I Average yields. The average yield from 1000 grams of wax is approximately? I Alcohbls i 50 gms. I-lydrocarbons gms. Fatty acids aa-. ......".I. .l. 300. gms.

Totaln is 450 gms. From the finished product, the three groups of substances, alcohols, hydrocarbone and fatty acids can be recovered in were used in the case of the original wax,

as herein described. As these substances are derived from bacteria of the various species of the genus zllyc'obaczerz'acew, I have designated the alcohols as mycol alcohols, the hydrocarbons as mycolenes, and the fatty acids as mycoleic acids.

These derivatives obtained from the wax of the acid-fast bacteria, when injected separately or mixed together into the host, attack the wax elaborated by the bacilli therein so as to dissolve or digest or catabolize or destructively change: the same.

I claim and desire to obtain by Letters Patent the following:

1. A substance comprising a derivative of a compound contained in the wax elaborated by acid-fast bacilli containing only organic radicals having therapeutic action upon the host containing the acid-fast bacilli when administered parenterically.

2. A substance comprising a derivative of a compound contained in the wax elaborated by tubercle bacilli containing only organic radicals having therapeutic action upon the host containing acid-fast bacilli when administered parentcrically.

3. A substance comprising a derivative of a compound contained in the wax elaborated by acid-fast bacilli containing only organic radicals capable of hypodermic injection without caseation.

at. A substance comprising a derivative of a compound contained in the wax elaborated by tubercle bacilli containing only organic radicals capable of hypodermic injection without caseation. v t

5. A substance comprising an ester derivative ofa'fatty acid contained in the wax elaborated by acid-fast bacilli having therapeutic action upon the host containing acidfast bacilli when administered parenterically.

6. A substance comprising an ester derivative of a fatty acid contained in the wax elaborated by tubercle bacilli having therapeutic action upon the host containing acidfast bacilli when administered parenteri cally.

7. A substance comprising an ethyl ester of a fatty acid contained in the wax elaborated by acid-ta bacilli having therapeutic action upon the host containing acidfast bacilli when administered parenteri- .cally. I

8. A substance comprising an ethyl ester of a fatty acid contained in the ax elaborated by tubercle bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parentcrically.

9. A substance comprising an ester derivative of an alcohol. contained in the wax elaborated by acidfast bacilli having thereapeutic action upon the host containing acidfast bacilli when administered parenterically.

10, A substance comprising an ester derivative of an alcohol contained in the wax elaborated by tubercle bacilli having thera peutic action upon the host containing acidfast bacilli vwhen administered parenterically.

11. A substance comprising an acetic ester of an alcohol contained in the wax elaborated by acid-fast bacilli having therapeutic action'upon the host containing acidfast bacilli when administered parenteri- 'ally.

12. A substance comprising an acetic ester of an alcohol contained in'the wax elaborated by tubercle bacilli having therapeutic action upon the host containing acidfast bacilli when administered parenterically.

13. A substance comprising an ester derivative of a hydrocarbon contained in the wax elaborated by acid-fast bacilli hav ing therapeutic action upon the host containing acidfast bacilli when administered parenterically. v

ll. A substance comprising an ester derivative of a hydrocarbon contained in the wax elaborated by tubercle bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parenterically.

15. A substance comprising a salicylic ester of a hydrocarbon contained in the av elaborated by acid-fast bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parenterically.

16. A substance comprising a salicylic ester of a hydrocarbon contained in the wax elaborated byctuberclc bacilh having therapeutic action upon the host containing acidfast bacilli when administered parenterically.

of a. compound contained in the wax elaborated by not-highly-virulent acid-fast bacilli having therapeutic action upon the host containing acid-fast bacilli when administered j'mrenterically.

18. A substance comprising a derivative of a compound contained in the wax elaborated. by not-high]y-virulent acid-fast bacilli 17. A substance comprising a derivative capable ct hypodermic injection without caseati'on.

1th A substance comprising an ester derivative of analcohol and an ester derivative of a hydrocarbon contained in" the wax elaborated by acid-fast bacilli havingtherapeutic action uponthe host containingacidpare'nteria fatty acid contained in the wax elaborated by acid-fast bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parenterically.

'22. A substance comprising an ester derivative of an alcohol, an ester derivative of a hydrocarbon and an ester derivative of a fatty acid contained in the Wax elaborated by tubercle bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parenterically.

23. A substance comprising an ester deriva-tive of an unsaturated hydrocarbon contained in the wax elaborated by acid-fast bacilli having therapeutic action upon the host containing acid-fast bacilli when administered parenterically.

24. A substance comprising an ester derivative of an unsaturated hydrocarbon contained in the wax elaborated by tubercle bacilli having therapeutic action upon the host containing acid-fast bacilli when ad,

ministered parent'erically.

. 25. The process winch comprises decomposing a compound contained in the wax elaborated by acid-fast bacilli and forming therefrom a derivative thereof containing only organic radicals.

26. The process which comprises saponifying a compound contained in. the was elaborated by acid-fast bacilli and estenfying the fatty acid thus obtained.

27. The process which comprises saponifying a compound contained in the wait elab orated 'by tubercle bacilli and esterifymg the fatty acid thus obtained.

' 28. The process which comprises saponifying a compound contalned in the wax elaborated'**by acidfast tacilli, removing the alcohols, and esterifying the fatty acid thus 29. The process which comprises saponifying a compound contained in the wax elaboratedby tubercle bacilli, removlng the alcohols, and esterifying the fatty acid thus obtained.

30. The process which comprises saponifying a compound contained in the Wax elaborated by acid-fast bacilli, removing the alcohols and hydrocarbons, and esterifying the fatty acid thus obtained. i 31. The process which comprises saponifying a compound contained in the wax elaborated by tubercle bacilli, removin the alcohols and hydrocarbons, and esteri ying the fatty acid thus obtained.

32. The process which comprises saponi- ,fying a compound contained in the wax elaborated by acid-fast bacilli, removing the alcohol and hydrocarbons, decanting and esterifying the fatty acid thus obtained.

33. The process which comprises saponifying a compound contained in the wax elaborated by tubercle bacilli, removing the alcohols and hydrocarbons, decanting, and esterifying the fatty acid thus obtained.

34:. The process which comprises saponifying a compound contained in the wax elaborated byacid-fast bacilli, removing an alcohol, esterifying the alcohol, and esteri-v 36. The pl'OCBS'SWlllch comprises saponifying a compound contained in the wax elaborated by acid-fast bacilli, removing an alcohol, esterifyin'gthe alcohol, separating a hydrocarbon therefrom, and esterifying the fatty acid thus obtained.

'37. The process which comprises saponifying a compound contained in the wax elaborated by tubercle bacilli, removing an alcohol, esterifying the alcohol, separating a hydrocarbon therefrom, andesterifying the fatty acidthus obtained.

38. The process which comprises saponifying a compound contained in the wax elaborated by acid-fast bacilli, removing an alcohol, esterifying the alcohohseparating a hydrocarbon therefrom, esterifying the hydrocarbon, and esterifying the fatty acid .thus obtained.

39. The process which comprisessaponifying a compoundcontained in the wax elaboratedby tubercle bacilli, removing an alcohol, esterifying the alcohol, separating a hydrocarbon therefrom, esterifying the hydrocarbon, and esterifyingthe fatty acid thus obtained.

10. The process which comprises saponifying a compound contained in the wax.

elaborated by acid-fast bacilli, removingan 42. The process which comprises saponifyinga compound contained in the wax elaborated by acid-fast bacilli, removing an alcohol, and esterifying the alcohol.

43. The process which comprises saponifying a compound contained in the Wax elaboratedby tubercle bacilli, removing an alcohol, and esterifying the alcohol.

44. The process which. comprises saponifying a compound contained in the wax elaborated by acid-fast bacilli, removingan alcohol, esterifying the alcohol, and separating a hydrocarbon therefrom.

45. The process which comprises saponi-- fying a compound contalned 1n the waxy elaborated by tubercle bacilli, removing an alcohol, esterifying the alcoliol, and separating a hydrocarbon therefrom.

46. Theprocess which comprises saponifying a compound contained in the wax elaborated by acid-fast bacilli, removing an alcohol, esterifying the alcohol, separating a. hydrocarbon therefrom, and esterifying the hydrocarbon.

47. The prccess which comprisessaponifying a' compound contained in the Wax elaborated by tubercle bacilli, removing an alcohol, esterifying the-alcohol, separating a hydrocarbon therefrom, and esterifying the hydrocarbon.

. 48'. The process which comprises saponifying a compound contained in the wax elaborated by acid-fast bacilli, removing an Copies 91' thls patent may be obtained {or live cent! each,-by addressing the"commllsioner.ct Patents.

alcohol, esterifyingk the alcohol, separating a hydrocarbon therefrom, and esterifying the hydrocarbon to form a salicylate.

49. The process which comprises saponif'ying a compound contained in the Wax elaborated by tubercle bacilli, removing an alcohol, esterifying the alcohol, separating a hydrocarbon therefrom,-and esterifying the hydrocarbon to form a salicylate.

50. The process which comprises saponi fying a compound contained in the Wax elaborated by acid-fast bacilli, removing'an alcohol, esterifying the alcohol, separating specification in the presence of two subscribing witnesses.

BENJAMIN S. PASOHALL.

Witnesses;

EDWARD L. OAKES, I. R. SHARK.

Washington, D. 0.

It is hereby certified that in Letters Patent No. 1,250,345, granted December 18, 1917, upon the application of Benjamin S. Paschell, of Seattle, Washington. for an improvement in Substances for Treatment of Tuberculosis, Leprosy, and

Other Diseases and Processes of Mixing Said Substances, an error appears in the printed specification requiring correction as follows: Page 8,1ine 24, claim 1, strike out the article the; and that the said Letters Patent should be read with this correction therein that the same may conform to the record of the case in the Patent Ofiice.

Signed and sealed this 12th day of March, A. D., 1918.

[sun] R. F. WHITEHEAD,

Acting Commissioner of Patents. Cl. 1s7 7. 

